CAS 170157-64-9: Boc-.beta.-(2-quinolyl)-D-Ala-OH

Description: Boc-β-(2-quinolyl)-D-Ala-OH is a chemical compound characterized by its structure, which includes a tert-butyloxycarbonyl (Boc) protecting group, a β-amino acid moiety, and a quinoline ring. The presence of the Boc group indicates that this compound is likely used in peptide synthesis, as it serves to protect the amino group during chemical reactions. The β-(2-quinolyl) component suggests that the compound may exhibit unique biological activities or interactions due to the quinoline's aromatic nature and potential for coordination with metal ions. The D-Ala (D-Alanine) portion indicates that this compound is an enantiomer of alanine, which can influence its biological properties and interactions in various biochemical pathways. Overall, Boc-β-(2-quinolyl)-D-Ala-OH is of interest in medicinal chemistry and peptide synthesis, potentially serving as a building block for more complex molecules or as a tool for studying biological processes involving amino acids and their derivatives.

Formula: C₁₇H₂₀N₂O₄

Synonyms:

• Boc-D-2-Quinoylalanine

BOC-β-(2-QUINOLYL)-D-ALA-OH

CAS: 170157-64-9

• Formula: C₁₇H₂₀N₂O₄
• Purity: 95%
• Color and Shape: Solid
• Molecular weight: 316.3517

(R)-2-((tert-Butoxycarbonyl)amino)-3-(quinolin-2-yl)propanoic acid

CAS: 170157-64-9

• Purity: 95.0%
• Molecular weight: 316.35699462890625

Boc-3-(2'-quinolyl)-D-alanine

CAS: 170157-64-9

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• Formula: C₁₇H₂₀N₂O₄
• Purity: Min. 95%
• Molecular weight: 316.35 g/mol